AVID Medical Recalls Robotic Prostatectomy Pack Due to Discoloration

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Recalling firmAVID Medical, Inc.9000 Westmont Dr, N/A · Toano, VA 23168-9351

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✎ GovInfoNow plain-language explainer

What happened, in plain English

AVID Medical is recalling robotic prostatectomy packs that may have discoloration due to improper resterilization. This could affect visualization during surgery, though the risk is not described as causing injury.

Why it’s dangerous

The visualization system in the packs was resterilized incorrectly, causing discoloration. This could potentially impair the surgeon's ability to see the surgical field clearly during procedures.

Who’s affected

Surgical teams using the AVID robotic prostatectomy packs for prostate removal procedures. Patients undergoing surgery with these kits may be at risk if discoloration affects visualization.

How to tell if you have this one

Check for model number NAMC423-08 and lot numbers 1624611, 1624612, or 1628010. The kits were sold with a unique device identifier (UDI) 10809160374627.

Brand
AVID Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Lot Number
Look for lot numbers 1624611, 1624612, or 1628010 on the packaging.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The visualization system was inadvertently resterilized, causing discoloration that may impair surgical visualization.

Is there a risk of injury from this discoloration?

The recall record does not state that discoloration causes injury; it only mentions potential visual impairment during surgery.

How can I check if my pack is affected?

Check for model number NAMC423-08 and lot numbers 1624611, 1624612, or 1628010.

Take action

Contact AVID Medical

We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2262-2025 — AVID Medical AVID Medical

Hello,

I own a AVID Medical that is covered by recall Z-2262-2025 from AVID Medical.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2262-2025 (June 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2262-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.

Lower-risk recall